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Illumina at ESHG 2017

777 views | 7 years ago

A global genomics leader, Illumina provides comprehensive next-generation sequencing solutions to the research, clinical, and applied markets. Illumina technology is responsible for generating more...

Insights into Index Hopping | Illumina Webinar

6050 views | 8 years ago

In this webinar Gary Schroth, PhD gives an introduction to index hopping, explains how to minimize index hopping levels by following best library practices, and discusses how to remove index-hopped...

Greater Good Initiative 2017

408 views | 8 years ago

Since 2011, the Agricultural Greater Good Initiative has awarded grants to researchers using Illumina technology to help alleviate global hunger, malnutrition, and poverty. The 2017 grant was awarded...

Building a reference genome for Nelore cattle

882 views | 8 years ago

Dr Fernando Garcia, Professor of genomics at Sao Paulo State University, discusses the significance of building a reference genome for Bos indicus Nelore cattle. Garcia shares the role next-generation...

Insights into Index Hopping | Illumina Webinar

445 views | 8 years ago

In this webinar Gary Schroth, PhD gives an introduction to index hopping, explains how to minimize index hopping levels by following best library practices, and discusses how to remove index-hopped...

The Illumina Bio-Rad Single Cell Sequencing Solution

4795 views | 8 years ago

Profile transcriptomes of hundreds to tens of thousands of single cells with the Illumina Bio-Rad Single-Cell Sequencing Solution, a robust and scalable high-throughput next-generation sequencing (NGS)...

Next generation sequencing-based analyses of hematological malignancies.

1204 views | 8 years ago

Professor Christian Thiede describes the work his lab at the University Hospital Carl Gustav Carus in Dresden, Germany, using NGS to address the complex molecular genetics of hematological malignancies....

Identification of Novel Fusions and Pharmacogenomic Targets in Cancer

595 views | 8 years ago

This webinar describes the optimization and validation of two commercially available clinical research next-generation sequencing (NGS) assays. The first assay is aimed at identifying fusion transcripts...